key: cord-0025901-v2f8onhn
authors: Butler, Javed; Filippatos, Gerasimos; Jamal Siddiqi, Tariq; Brueckmann, Martina; Böhm, Michael; Chopra, Vijay K.; Pedro Ferreira, João; Januzzi, James L.; Kaul, Sanjay; Piña, Ileana L.; Ponikowski, Piotr; Shah, Sanjiv J.; Senni, Michele; Vedin, Ola; Verma, Subodh; Peil, Barbara; Pocock, Stuart J.; Zannad, Faiez; Packer, Milton; Anker, Stefan D.
title: Empagliflozin, Health Status, and Quality of Life in Patients With Heart Failure and Preserved Ejection Fraction: The EMPEROR-Preserved Trial
date: 2021-11-15
journal: Circulation
DOI: 10.1161/circulationaha.121.057812
sha: 753e1909ac98a603787125c6d1bcb7c762684b4d
doc_id: 25901
cord_uid: v2f8onhn

BACKGROUND: Patients with heart failure with preserved ejection fraction have significant impairment in health-related quality of life. In the EMPEROR-Preserved trial (Empagliflozin Outcome Trial in Patients With Chronic Heart Failure With Preserved Ejection Fraction), we evaluated the efficacy of empagliflozin on health-related quality of life in patients with heart failure with preserved ejection fraction and whether the clinical benefit observed with empagliflozin varies according to baseline health status. METHODS: Health-related quality of life was measured with the Kansas City Cardiomyopathy Questionnaire (KCCQ) at baseline and 12, 32, and 52 weeks. Patients were divided by baseline KCCQ Clinical Summary Score (CSS) tertiles, and the effect of empagliflozin on outcomes was examined. The effect of empagliflozin on KCCQ-CSS, Total Symptom Score, and Overall Summary Score was evaluated. Responder analyses were performed to compare the odds of improvement and deterioration in KCCQ related to treatment with empagliflozin. RESULTS: The effect of empagliflozin on reducing the risk of time to cardiovascular death or heart failure hospitalization was consistent across baseline KCCQ-CSS tertiles (hazard ratio, 0.83 [95% CI, 0.69–1.00], 0.70 [95% CI, 0.55–0.88], and 0.82 [95% CI, 0.62–1.08] for scores <62.5, 62.5–83.3, and ≥83.3, respectively; P trend=0.77). Similar results were seen for total heart failure hospitalizations. Patients treated with empagliflozin had significant improvement in KCCQ-CSS versus placebo (+1.03, +1.24, and +1.50 at 12, 32, and 52 weeks, respectively; P<0.01); similar results were seen for Total Symptom Score and Overall Summary Score. At 12 weeks, patients on empagliflozin had higher odds of improvement ≥5 points (odds ratio, 1.23 [95% CI, 1.10–1.37]), ≥10 points (odds ratio, 1.15 [95% CI, 1.03–1.27]), and ≥15 points (odds ratio, 1.13 [95% CI, 1.02–1.26]) and lower odds of deterioration ≥5 points in KCCQ-CSS (odds ratio, 0.85 [95% CI, 0.75–0.97]). A similar pattern was seen at 32 and 52 weeks, and results were consistent for Total Symptom Score and Overall Summary Score. CONCLUSIONS: In patients with heart failure with preserved ejection fraction, empagliflozin reduced the risk for major heart failure outcomes across the range of baseline KCCQ scores. Empagliflozin improved health-related quality of life, an effect that appeared early and was sustained for at least 1 year. REGISTRATION: URL: https://www.clinicaltrials.gov; Unique identifier: NCT03057951.

A pproximately half of all patients with heart failure (HF) have preserved ejection fraction (HFpEF). 1, 2 Not only do patients with HFpEF experience similar risk for adverse clinical outcomes compared with those with HF with reduced ejection fraction, but also both HF phenotypes have similarly impaired physical functioning and health-related quality of life (HRQoL). 3, 4 Although the overall burden of impaired HRQoL is similar in both HF with reduced ejection fraction and HFpEF, most of the data related to health status in HF have been derived from patients with HF with reduced ejection fraction. 5, 6 The EMPEROR-Preserved trial (Empagliflozin Outcome Trial in Patients with Chronic Heart Failure with Preserved Ejection Fraction) studied the sodium glucose cotransporter-2 inhibitor empagliflozin in patients with HFpEF and a left ventricular ejection fraction >40% and showed a significant reduction in the risk of cardiovascular death or HF hospitalization. 7 The overall patient's health status, including HRQoL, in the EMPEROR-Preserved trial was assessed with the Kansas City Cardiomyopathy Questionnaire (KCCQ), providing an opportunity to understand the impact of baseline HRQoL on clinical benefits with empagliflozin and, conversely, the effect of empagliflozin on HRQoL.

The design and primary results of the EMPEROR-Preserved trial have been published previously. 6 In brief, the EMPEROR-Preserved trial was a phase III international, multicenter, randomized, double-blind, parallel-group, placebo-controlled trial that enrolled adult patients who had chronic HF with New York Heart Association class II to IV symptoms for at least 3 months and a left ventricular ejection fraction of >40% with no previous measurement of ≤40% under stable conditions. Patients were required to have elevated NT-proBNP (N-terminal pro-B-type natriuretic peptide) levels (>900 pg/mL or >300 pg/mL in patients with or without atrial fibrillation, respectively) and evidence of structural heart disease (left ventricular hypertrophy or left atrial enlargement) or a documented hospitalization for HF within the 12 months before enrollment. The protocol was approved by the ethics committee of each of the 622 participating sites in 23 countries, and all patients gave written informed consent. summarized as (1) Total Symptom Score (TSS), which consists of symptom frequency and symptom burden domains;

(2) Clinical Summary Score (CSS), consisting of physical limitation and TSS; and (3) Overall Summary Score (OSS), which is formed by combining CSS, quality of life, and social limitation domains. The scores range from 0 to 100, with 100 being the best possible score. The KCCQ has been shown to be valid, reliable, and sensitive to clinical changes, and lower KCCQ scores are associated with higher risk of hospitalizations and mortality. [8] [9] [10] The KCCQ was completed by patients at baseline and at 12, 32, and 52 weeks after randomization to placebo or empagliflozin.

Study participants were categorized according to tertiles of baseline KCCQ-CSS, KCCQ-TSS, and KCCQ-OSS. Baseline characteristics were summarized as frequencies and percentages or means with SDs. The effect of empagliflozin in each tertile was assessed by hazard ratios with 95% CIs using a Cox proportional hazard model, accounting for noncardiovascular death as a competing risk. In addition, the effect of empagliflozin on total (first and recurrent) hospitalizations for HF in KCCQ tertiles was analyzed by a joint frailty model with cardiovascular death as a competing risk.

To assess the affect of empagliflozin on HRQoL, differences between treatment groups in mean KCCQ-CSS, KCCQ-TSS, and KCCQ-OSS at 12, 32, and 52 weeks were calculated with a mixed model for repeated measures, and the least-squares mean difference between treatment groups was estimated after adjustment for baseline KCCQ score, estimated glomerular filtration rate, age, region, sex, diabetes status, and left ventricular ejection fraction. Responder analyses were performed to investigate the proportion of patients with an improvement or deterioration in KCCQ score at 12, 32, and 52 weeks after randomization; established clinically meaningful thresholds for changes in KCCQ (≥5, ≥10, and ≥15 points for improvement and ≥5 point for deterioration) were used for all responder analyses.

Multiple imputation was used to account for missing KCCQ values, and estimates were combined by use of the Rubin rules. 11 Odds ratios with 95% CIs were calculated from a logistic regression model, which included baseline KCCQ score, estimated glomerular filtration rate, age, region, sex, diabetes status, and ejection fraction as covariates. Patients who died before 12, 32, and 52 weeks were counted as not improved in the analyses of improvement and as worse in the analyses of deterioration. To accommodate for the fact that patients with a very high baseline KCCQ score are not able to experience certain numeric improvements, patients with baseline KCCQ values of ≥95, ≥90, or ≥85 points in KCCQ domains were considered to have 5-, 10-, or 15-point improvement, respectively, if their values remained ≥95, 90, or 85. Similarly, patients with a KCCQ score ≤5 points at baseline were defined as deteriorated if their score remained ≤5 points. All analyses were conducted with SAS version 9.4 (SAS Institute, Cary, NC).

The sponsor of the EMPEROR-Preserved trial (Boehringer Ingelheim) is committed to responsible sharing of clinical study reports, related clinical documents, and patient-level clinical study data. Researchers are invited to submit inquiries via the Boehringer Ingelheim website.

Among the 5942 participants with a baseline KCCQ assessment, the mean (SD) KCCQ-CSS, KCCQ-TSS, and KCCQ-OSS were 70.4 (21.2), 73.5 (22.0), and 68.9 (21.1), respectively. Baseline characteristics of patients in KCCQ-CSS tertiles are shown in Table 1 . Patients with lower KCCQ-CSS were more often female and White, were more often enrolled in Europe, and were more likely to have worse New York Heart Association class, higher body mass index and NT-proBNP levels, and a history of diabetes and atrial fibrillation. An overview of the availability of KCCQ-CSS data at each time point is shown in Figure S1 . 

The adjusted mean change in KCCQ-CSS, KCCQ-TSS, and KCCQ-OSS by treatment arms over time is presented in Figure 2A through 2C. Compared with those treated with placebo, patients treated with empagliflozin had a significant improvement in mean KCCQ score at 12, 32, and 52 weeks: CSS, 1.03, 1.24, and 1.50 points; TSS, 1.77, 1.53, and 2.07 points; and OSS, 1.10, 1.53, and 1.60 points, respectively (P<0.01 for all; Figure 3 ). The effect of empagliflozin on KCCQ-CSS, KCCQ-TSS, and KCCQ-OSS by tertiles of baseline score at 12, 32, and 52 weeks is shown in Table 2 (Figures 4 and 5) . Data are mean (SD) when appropriate. Race was self-reported. Those who identified with >1 race or with no race were classified as "other. " ARB excludes valsartan when taken with sacubitril because sacubitril/valsartan is shown as an ARNI.

ACE indicates angiotensin-converting enzyme; ARB, angiotensin receptor blocker; ARNI, angiotensin receptor neprilysin inhibitor; BMI, body mass index; eGFR, estimated glomerular filtration rate; HF, heart failure; KCCQ-CSS, Kansas City Cardiomyopathy Questionnaire Clinical Summary Score; and NT-proBNP, N-terminal pro-B-type natriuretic peptide.

*Excluding mineralocorticoid receptor antagonists.

In this prespecified analysis of the EMPEROR-Preserved trial, we show 2 key findings. First, empagliflozin reduced the risk for major HF outcomes in patients with HFpEF across the entire range of baseline HRQoL. Second, em-pagliflozin improved HRQoL, and the improvement was seen early and was sustained for at least 1 year. Patients treated with empagliflozin were more likely to show clinically meaningful improvement and less likely to experience clinically meaningful deterioration in health status compared with patients treated with placebo. These findings are highly concordant with those reported with empagliflozin in patients with a reduced ejection fraction (≤40%) who were enrolled in the EMPEROR-Reduced trial (Empagliflozin Outcome Trial in Patients With Chronic Heart Failure With Reduced Ejection Fraction). 5 Together, these data suggest that empagliflozin improves HRQoL across a broad range of patients with HF. Several studies have assessed the effect of treatment on health status in patients with HFpEF. [12] [13] [14] [15] [16] [17] The TOPCAT trial (Treatment of Preserved Cardiac Function Heart Failure With an Aldosterone Antagonist) with 3400 patients showed a baseline mean KCCQ-OSS of 54.8 and demonstrated a 1.36-point improvement over placebo at 4 months. 12 The PARAGON-HF trial (Prospective Comparison of ARNI With ARB Global Outcomes in HFpEF) enrolled patients with a baseline health status similar to that in EMPEROR-Preserved (mean KCCQ-CSS, 74.2) and showed an improvement in KCCQ-CSS with sacubitril/valsartan by 1.0 point compared with placebo at 8 months. 13 Several smaller trials have also assessed the effect of treatments on KCCQ in patients with HFpEF. The VITALITY-HFpEF trial (Patient-Reported Outcomes in Vericiguat-Treated Patients With HFpEF) showed no improvement in KCCQ with vericiguat. 14 In the NEAT-HFpEF trial (Nitrate's Effect on Activity Tolerance in Heart Failure With Preserved Ejection Fraction), treatment with isosorbide mononitrate showed numerically (although not statistically significant) unfavorable changes in KCCQ scores. 15 The EMPERIAL-Preserved trial (Empagliflozin Outcome Trial in Patients With Chronic Heart Failure With Preserved Ejection Fraction) did not show a significant effect of empagliflozin on KCCQ-TSS in a 12-week trial in ≈300 mildly symptomatic patients with HFpEF. 17 In contrast, the PRESERVED-HF trial (Dapagliflozin in Preserved Ejection Fraction Heart Failure) showed a significant improvement in the KCCQ-CSS with dapagliflozin in patients with HFpEF 16 ; the trial enrolled patients with obesity in the United States with >40% having New York Heart Association class III to IV symptoms.

The magnitude of the treatment effect on KCCQ health status seen in the EMPEROR-Preserved trial may appear to be modest (1.0-2.0 points) compared with a change of 5.0 points, which is commonly regarded as representing a clinically meaningful shift in KCCQ scores. However, the 5-point threshold change has been identified as meaningful in individual patients rather than in populations of patients. 18 In population studies, it may be difficult to achieve a 5-point between-group difference, especially if the baseline KCCQ score is >70, indicative of a reasonably good quality of life and health status. Large betweengroup differences in KCCQ scores (eg, 10-to 15-point treatment effects) have typically been observed only in patients who were severely compromised at baseline and particularly in unblinded device trials, in which knowledge that a patient has received active therapy likely exaggerated changes in their perception of their own response to an experimental intervention. 19 Decisions about the handling of missing data and imputation methods may also amplify the size of a treatment difference. It is therefore noteworthy that the magnitude of the treatment effect 20 Our analyses and findings should be considered in light of certain strengths and limitations. The current study is the largest trial to evaluate the effect of any treatment on health status and quality of life, and our data were complete through 1 year in nearly 90% of patients. Longer-term data were not collected in this trial, but it is often difficult to interpret data beyond 12 months because of competing risks of deaths and other serious events. Furthermore, we studied stable patients who primarily had functional class II symptoms, and treatment effects may have differed if we had enrolled patients with greater degrees of disability and limitation at the start of the trial. Finally, the current analysis did not evaluate and TSS, total symptom score the influence of ejection fraction or sex on the effect of empagliflozin on KCCQ scores because these analyses are being presented fully in other publications. If brief, we previously reported an attenuated response for the effect of empagliflozin on HF hospitalizations in patients with ejection fractions ≥60% to 65%, 20 and we noted an attenuated effect of empagliflozin on KCCQ scores in patients with the highest ejection fractions. In contrast, sex did not influence the effect of empagliflozin on KCCQ scores in the EMPEROR-Preserved trial, whereas in the PARAGON-HF trial, KCCQ scores in men responded significantly more favorably to sacubitril/valsartan than KCCQ scores in women. 21 

Treatment with empagliflozin reduced the risk for cardiovascular death or HF hospitalization across the range of baseline HRQoL scores in patients with HFpEF. Empagliflozin also significantly improved HRQoL in patients 

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The authors were fully responsible for all content and editorial decisions, were involved at all stages of development, and have approved the final version. Graphical assistance was supported financially by 7 

Expanded Methods Figures S1 and S2